Sensation Plus 8Fr 50cc Intra-Aortic Balloon Catheter
Recall
- Recall Number
- Z-1686-2022
- Event Number
- 90684
- Firm
- Datascope Corporation
- FEI Number
- 1000222374
- Product Code
- DSP
- Status
- Open, Classified
- Root Cause
- Vendor change control
- Initiated
- August 5, 2022
- Posted
- September 8, 2022
- Address
- 15 Law Dr, Fairfield, NJ, 07004-3206
Description
Sensation Plus 8Fr 50cc Intra-Aortic Balloon Catheter
Certain lots containing undersized dilator.
The firm distributed an Urgent Medical Device Removal notification, by mail, dated August 5, 2022. The notification informs customers that certain lots of 8Fr. 50cc IAB catheter and insertion kits are being recalled due to an undersized vessel dilator. During a sheathless insertion, the undersized inner diameter may result in the inability to insert the guidewire through the inner lumen of the dilator and the undersized outer diameter may reduce dilation of the vessel. If used in a procedure, recalled product could result in a procedural delay, gas emoli, and vessel injury. Customers are asked to examine their inventory to determine if they have nay recalled product and to quarantine any affected units. Customers with recalled product are to contact Datascope Corp./Getinge Customer Service at 888-9GETUSA (888-943-8872, option 2) between the hours of 8 AM and 6 PM to request a return authorization number to receive full credit. Distributors who have shipped any product are to forward the notification to customers. The recall notification is to be forwarded to all users at hospitals/facilities. Customers are asked to complete and return the recall response form by email to [email protected] or by fax to 877-647-1921.
Awaiting domestic distribution. Foreign: Australia, Belgium, Canada, Czech Republic, France, Germany, Hong Kong, Iceland, Ireland, Italy, Netherlands, New Zealand, Norway, Poland, Portugal, Saudi Arabia, Slovenia, South Africa, Spain, Sweden, Switzerland, United Arab Emirates, United Kingdom.
10,427 units